If your ASCP prep feels dry and chaotic, you’re studying wrong 🤷🏽‍♀️ Join the CLS crew that actually gets RESULTS. Weekly study sessions, wild memory hacks, and the most fun you’ve ever had prepping for the ASCP. Link in bio. Get ASCP Certified already!🔬📚💅🏽 #ascp #testprep #medtech #healthcare #study | Marilyn Claire
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If your ASCP prep feels dry and chaotic, you’re studying wrong 🤷🏽‍♀️ Join the CLS crew that actually gets RESULTS. Weekly study sessions, wild memory hacks, and the most fun you’ve ever had prepping for the ASCP. Link in bio. Get ASCP Certified already!🔬📚💅🏽 #ascp #testprep #medtech #healthcare #study | Marilyn Claire
20.3K views10 months ago
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Day 9 🧪 Welcome to 30 Days of ASCP: Ratchet Study Tips🤪🤏🏽🤏🏽🤏🏽 Today we’re finally clearing up reactive lymphocytes vs monocytes: the cells everybody loves to mix up on diff counts. The secret is chromatin first: reactive lymphs usually have fine chromatin and may show a visible nucleolus(especially immunoblasts), but not all reactive lymphs will have one, so don’t rely on that alone. They often have light to pale blue cytoplasm that hugs surrounding RBCs. Monocytes do not have nucleoli,
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Day 9 🧪 Welcome to 30 Days of ASCP: Ratchet Study Tips🤪🤏🏽🤏🏽🤏🏽 Today we’re finally clearing up reactive lymphocytes vs monocytes: the cells everybody loves to mix up on diff counts. The secret is chromatin first: reactive lymphs usually have fine chromatin and may show a visible nucleolus(especially immunoblasts), but not all reactive lymphs will have one, so don’t rely on that alone. They often have light to pale blue cytoplasm that hugs surrounding RBCs. Monocytes do not have nucleoli,
23.2K views4 months ago
FacebookMarilyn Claire
If you’ve ever opened your ASCP study materials and felt completely overwhelmed like, where do I even start? You are not alone. 🫶🏽😩 There’s so much content between blood bank, heme, micro, immuno, and chemistry that it can feel like you’re drowning before you even begin. The reality is, you don’t need to know everything at once; you need a structured starting point. Begin with a baseline full-length practice exam to pinpoint your weakest subject, then work backwards from weakest to strongest,
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If you’ve ever opened your ASCP study materials and felt completely overwhelmed like, where do I even start? You are not alone. 🫶🏽😩 There’s so much content between blood bank, heme, micro, immuno, and chemistry that it can feel like you’re drowning before you even begin. The reality is, you don’t need to know everything at once; you need a structured starting point. Begin with a baseline full-length practice exam to pinpoint your weakest subject, then work backwards from weakest to strongest,
12.8K views6 months ago
FacebookMarilyn Claire
Day 16 🧪 Welcome back to 30 Days of ASCP: Ratchet Study Tips. 🤪🤏🏽 🤏🏽 🤏🏽 Platelet disorders stop being confusing once you separate the problem into three categories: too few, not working, or being destroyed. Thrombocytopenia is the obvious one; low platelets, less clotting, more bleeding. That can come from decreased production, increased destruction, or sequestration, and the smear will usually tell you which direction to look. Qualitative disorders are the sneaky ones, platelet count is
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Day 16 🧪 Welcome back to 30 Days of ASCP: Ratchet Study Tips. 🤪🤏🏽 🤏🏽 🤏🏽 Platelet disorders stop being confusing once you separate the problem into three categories: too few, not working, or being destroyed. Thrombocytopenia is the obvious one; low platelets, less clotting, more bleeding. That can come from decreased production, increased destruction, or sequestration, and the smear will usually tell you which direction to look. Qualitative disorders are the sneaky ones, platelet count is
4.3K views3 months ago
FacebookMarilyn Claire
Day 8 🧪 Welcome back to 30 Days of ASCP: Ratchet Study Tips! 🍄🔬 Today we’re locking in the dimorphic fungi that LOVE to show up on exams:Coccidioides, Histoplasma, Blastomyces, and Paracoccidioides. From boxcar-shaped arthroconidia and spherules, to spiky tuberculate macroconidia, to lollipop conidia, to the mariner’s wheel in tissue; if you know the growth pattern, the spores, and the geography, these questions get a LOT easier. Save this for later, send it to your study partner, and follow
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Day 8 🧪 Welcome back to 30 Days of ASCP: Ratchet Study Tips! 🍄🔬 Today we’re locking in the dimorphic fungi that LOVE to show up on exams:Coccidioides, Histoplasma, Blastomyces, and Paracoccidioides. From boxcar-shaped arthroconidia and spherules, to spiky tuberculate macroconidia, to lollipop conidia, to the mariner’s wheel in tissue; if you know the growth pattern, the spores, and the geography, these questions get a LOT easier. Save this for later, send it to your study partner, and follow
4.9K views4 months ago
FacebookMarilyn Claire
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Day 9 🧪 Welcome back to 30 Days of ASCP: Make It Make Sense, because once you get it, you never forget it. Elution and adsorption are both used to separate antibodies from red blood cells, but they serve different purposes. Elution is used when an antibody is already attached to the patient’s red cells; we strip it off to identify what that antibody is, which is especially important in cases like positive DATs or hemolytic disease of the newborn. Adsorption is used when antibodies are free in t
4.9K views4 months ago
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Day 21🧪 Welcome back to 30 Days of ASCP: Make It Make Sense, because once you get it, you never forget it. CSF is collected in multiple tubes because each tube answers a different clinical question, and the order matters due to contamination during collection. Tube 1 is typically used for chemistry and serology because it may contain a small amount of blood contamination from the needle entering the space. Tube 2 is often used for microbiology, since sterility improves as collection continues.
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Day 16 🧪 Welcome back to 30 Days of ASCP: Make It Make Sense because once you get it, you never forget it. Today we’re breaking down SPEP, serum protein electrophoresis, and how to interpret patterns on the exam. SPEP separates serum proteins into five major fractions: albumin, alpha-1, alpha-2, beta, and gamma. What you’re really looking for are changes in the gamma region, where immunoglobulins live. A sharp, tall M-spike in the gamma region indicates a monoclonal protein: think multiple myel
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